Life Saving Drugs Program – Hereditary tyrosinaemia (type 1) – Medicines review protocol

This final protocol describes the methodology reviewers will follow to assess use of Life Saving Drugs Program medicines for hereditary tyrosinaemia (type 1).

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Life Saving Drugs Program – Hereditary tyrosinaemia (type 1) – Medicines review protocol

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Publication date:
Publication type:
Procedure
Audience:
General public
Language:
English
Description:

The reviewers will use data sources specified in this document and results of stakeholder consultation to describe:

  • prevalence of hereditary tyrosinaemia (HT1) in Australia
  • management of HT-1 in comparison to Life Saving Drugs Program (LSDP) guidelines
  • clinical and comparative effectiveness and safety of medicines
  • relevant patient-based outcomes
  • value for money of LSDP treatment for HT1
  • use of the LSDP HT1 medicines
  • developing technologies that may impact future access.

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